The Official Comment of AHRMM to the United States Department of Health and Human Services Food and Drug Administration (FDA) regarding Unique Device Identification for Medical Devices Docket No. FDA-2011-N-0090
AHRMM comments to the FDA regarding an amendment to the UDI proposed rule to address the UDI implementation time frame required by the 2012 Food and Drug Administration Safety and Innovation Act (FDASIA).
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The Patient Protection and Affordable Care Act of 2010 (ACA) requires the Secretary of Health and Human Services to establish a VBP program t
Letter/Comment
An announcement of the Final Rule issued by the IRS.
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In this page, AHRMM recommends these 3 proactive activities in the event of economic downturn.
Issue Brief
This learning lab covers alarm safety management in the health care supply chain field.
Toolkits/Methodology
How-to guide to managing IV disruptions.
Advisory
Guidance on Humidity Levels in the Operating Room